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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 37492Generated: October 25, 2026

Sodium Bicarbonate → 3,4-Diethoxycarbonyl-2-fluoro-5-nitro-6-phenylpyridine

https://huagongshe.com/reaction/37492

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
ReactantTrifluoroborane HydrofluorideHCID 9855450—
Reactant2-Amino-3,4-diethoxycarbonyl-5-nitro-6-phenylpyridineHCID 19935603—
ReactantSodium NitriteHCID 23668193—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
Product3,4-Diethoxycarbonyl-2-fluoro-5-nitro-6-phenylpyridineHCID 19935617—

Reaction Conditions

Temperature-5 °C

Reaction Steps

In 2 ml of acetic acid was dissolved 100 mg of 2-amino-3,4-diethoxycarbonyl-5-nitro-6-phenylpyridine, and 1.5 ml of 42% hydrofluoroboric acid was added to the solution. The mixture was cooled to -5° C., followed by adding dropwise a solution of 21 mg (1.1 eq) of sodium nitrite dissolved in 0.5 ml of water. Thirty minutes later, the temperature of the mixture was elevated to room temperature and the mixture was neutralized with sodium hydrogencarbonate, followed by extraction with ethyl acetate. After the organic layer was washed with water and a saturated aqueous solution of sodium chloride, and dried. After the solvent was distilled off, the resulting crystals (2-pyridone compound) were collected by filtration with hexane, and washed. The solvent was distilled off from the obtained filtrate, to give an oily substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05420275
Source datasetuspto-grants-1995_05
ORD IDord-4afe1d8998b646889314d45135528e41
Source noteuspto-grants-1995_05